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Circulation Research, ISSN 0009-7330, 07/2018, Volume 123, Issue 3, pp. 332 - 334
Mouse models have been invaluable for delineating the contributions of specific genes and signaling pathways to the pathogenesis of cardiac arrhythmias.... 
LEAK | atrial fibrillation | CARDIAC & CARDIOVASCULAR SYSTEMS | cell lines | oocytes | ATRIAL-FIBRILLATION MECHANISMS | gene targeting | PERIPHERAL VASCULAR DISEASE | HEMATOLOGY | mice | Animal models | Gene targeting | electrophysiology | animal models of human disease | Mouse models | Atrial fibrillation | Inherited arrhythmia disorders | gene therapy | Arrhythmias
Journal Article
Circulation research, ISSN 0009-7330, 2000, Volume 86, Issue 9, pp. E91 - E97
The congenital long-QT syndrome (LQT3) and the Brugada syndrome are distinct, life-threatening rhythm disorders linked to autosomal dominant mutations in... 
CARDIAC & CARDIOVASCULAR SYSTEMS | INHERITED CARDIAC-ARRHYTHMIA | Brugada syndrome | MECHANISM | SUDDEN-DEATH | Na+ channel | SODIUM-CHANNEL | long-QT syndrome | BRUGADA-SYNDROME | inactivation | SLOW INACTIVATION | PERIPHERAL VASCULAR DISEASE | MUTATIONS | HEMATOLOGY | ST SEGMENT ELEVATION | CANINE VENTRICULAR EPICARDIUM
Journal Article
Handbook of Experimental Pharmacology, ISSN 0171-2004, 2018, Volume 246, pp. 331 - 354
Journal Article
Journal Article
Journal Article
Journal of Arrhythmia, ISSN 1880-4276, 12/2017, Volume 33, Issue 6, pp. 572 - 578
Syncope, a common symptom of cerebral ischemia often shows a multifactorial etiopathogenesis. Although inherited arrhythmias causing syncope is uncommon, such... 
Inherited arrhythmia | Long QT syndrome | Catecholaminergic polymorphic ventricular tachycardia | Brugada syndrome | Syncope | Heart rate | Cardiac arrhythmia | Convulsions & seizures | Nuclear magnetic resonance--NMR | Congenital diseases | Electrocardiography | Cardiovascular disease | Family medical history | Mutation | Angina pectoris | Patients | Review
Journal Article